Compositions and Methods for Cartilage Repair

ABSTRACT

Autologous compositions and methods are provided for cartilage repair in patients in need thereof. Some aspects include combinations of platelet-based materials with chondrogenesis inducing agents in the presence or absence of cell-based therapies.

TECHNICAL FIELD

The invention generally relates to compositions and methods forcartilage repair in patients in need thereof. More particularly, theinvention relates to autologous compositions and methods for inducingchondrogenesis at sites in need of cartilage repair in patients in needthereof.

BACKGROUND

Mesenchymal stem cells are pluripotent blast or embryonic-like cellslocated in blood, bone marrow, dermis and perisosteum. In general, thesecells are capable of renewing themselves over extended periods of timeas well as, under various environmental conditions, differentiating intocartilage, bone and other connective tissue. Recently, variousinvestigators have researched the potential for using these cells torepair or regenerate target tissues, e.g., bone, cartilage, etc. In thismanner MSCs have been reported to have regenerative capabilities in anumber of animal models. See Acosta et al. (2005) Neurosurg Focus19(3):E4; Barry (2003) Novartis Found Symp. 249:86-102, 170-4, 239-41;Brisby et al. (2004) Orthop Clin. North Am. 35(1):85-89; Buckwalter andMankin (1998) Instr Course Lect. 47:487-504; Caplan (1991) J Orthop Res.9(5):641-650.

Recently, Centeno et al. (U.S. patent application Ser. No. 11/773,774)described a method for expanding MSC's using a growth channel andautologous platelet lysate. Also described were methods fortransplanting certain levels of growth factors (platelet lysate orplatelets) with the expanded MSC's to the area in a patient in need ofrepair. The levels of these growth factors were based on a percentage ofplatelet lysate needed to optimally expand the cells ex-vivo.

MSC's can readily differentiate in culture depending on cytokineexposure, environmental conditions (pressure, attachment opportunities,passage treatment, etc . . . ), or other chemical exposure. For example,exposure to varying levels of TGF-beta, FGF, and/or PDGF can all haveimpacts on the final cell phenotype produced in culture. In addition,leaving cells in culture longer also has impacts on differentiationpotential. Cells can be cultured for a certain visual morphology,confluence, or density, all of which has an impact on the final cellproduct produced and its potential for certain types of tissue repair.

In replacing or repairing tissue with MSC's, one concern is the use ofautologous or non-autologous cells. While MSC's have been traditionallyconsidered immune privileged, recent investigations have demonstratedtheir activation of the natural killer cell system in a foreign host.(Spaggiari, Capobianco et al. 2006) This makes the use of non-autologouscells difficult, as it is anticipated that the host's immune system willattack these foreign cells and potentially decimate the population oftransplanted MSCs, thus severely limiting their repair capabilities.

There is a need in the art for MSC expansion techniques that do not usedrugs or growth factors which are not FDA approved and can beeffectively used to replace tissue in a patient in need thereof. This isespecially true where the tissue in the patient in need of repair iscartilage. Cartilage repair is a major issue in health care which willonly continue to increase as the median age in the United Statescontinues to increase.

There is a need for autologous techniques to yield MSC and non-MSC basedcartilage repair techniques.

The present invention is directed toward overcoming one or more of theproblems discussed above.

SUMMARY OF THE EMBODIMENTS

The present invention provides repair compositions for facilitatingrepair and/or replacement of cartilage in patients in need thereof.Repair compositions include an effective amount of a platelet-basedmaterial in combination with one or more chondrogenesis inducing agents.In some cases the platelet-based material and/or the chondrogenesisinducing agent(s) are autologous.

Aspects of the platelet-based material include one or more of thefollowing solutions: platelet lysate, platelet rich plasma, plateletrich fibrin, and/or whole cell platelet concentrate.

Aspects of the chondrogenesis inducing agent include growth factors,cytokines, steroid hormones and nutrients for facilitating cartilageformation in patients in need thereof. One or more agents are combinedwith the platelet-based material. Chondrogenesis inducing agents can beautologous to the patient.

Repair compositions of the invention can further include cell-basedmaterials, including: mesenchymal stem cells, chondrocytes, isolatedbone marrow nucleated cells, chondrocyte progenitor cells, osteoblasts,embryonic stem cells, or stem cells of other lineages. Cells aretypically autologous to the patient, being harvested from the patientprior to cartilage repair and expanded to sufficient numbers for optimaltreatment.

Repair compositions of the invention can also include carrier materials,including: gels, hydrogels, absorbable polymers, and the like. Carriersact as scaffolding for cartilage formation within the site of cartilagerepair. Carriers can be added to the site of repair contemporaneouslywith the repair compositions or be part of the repair composition.

The present invention provides pharmaceutical compositions for use intherapeutic applications. Pharmaceutical compositions herein are used totreat patients having a site in need of cartilage repair, in some casesthe patient has osteoarthritis or other like degenerative disease.

The present invention provides kits having one or more of the followingmaterials: one or more platelet based material, one or morechondrogenesis inducing agent(s), one or more cell based material andone or more carrier. In some aspects the kit includes the materialsnecessary to harvest the target material from a patient rather than thematerial itself, for example the tools and supplies necessary to harvestand prepare a platelet lysate. Kits may include vials, tissue cultureflasks, culture medium, and other like laboratory materials necessaryfor the harvest and isolation of materials necessary to practice thepresent invention.

The present invention also provides methods for facilitating cartilagerepair or replacement in a patient in need thereof. Methods includeharvesting and preparing a platelet-based material, for example a 5% to40% platelet lysate, from a patient having a cartilage repair site inneed of treatment; optionally harvesting and preparing a chondrogenesisinducing agent from the same patient, e.g., isolating IGF-1 from thepatient, and/or obtaining and administering a non-autologouschondrogenesis inducing agent (such as dexamethasone, ascorbic acid, etc. . . ); optionally harvesting and preparing a cell-based therapy fromthe same patient, e.g., harvesting and isolating mesenchymal stem cellsfrom the patient's bone marrow, and/or obtaining and administering anon-autologous cell based material; optionally obtaining a carriermaterial; administering to the repair site a repair composition of theinvention; monitoring and re-administering repair compositions of theinvention to patient's that require additional treatment for cartilagerepair.

These and various features and advantages of the invention will beapparent from a reading of the following detailed description and areview of the appended claims.

DETAILED DESCRIPTION Definitions

The following definitions are provided to facilitate understanding ofcertain terms used frequently herein and are not meant to limit thescope of the present disclosure.

“About” refers to a +/−10% variation from the nominal value. It is to beunderstood that such variation is always included in any given valueprovided herein, whether or not it is specifically identified.

“Chondrogenesis inducing agent” refers to any agent capable of inducingor facilitating cartilage formation above the levels of cartilageformation found in a normal and untreated subject. Chondrogenesisinducing agents include but are not limited to; growth factors,cytokines, hormones, and various essential nutrients. Illustrativegrowth factors include Transforming Growth Factor-beta (TGF-β),Fibroblast Growth Factors (FGFs), Insulin Like Growth Factors (IGFs),Bone Morphogenic Proteins (BMPs); illustrative cytokines includingCytokine-like 1 (Cyt11); illustrative hormones include Human GrowthHormone (HGH); and Testosterone and illustrative essential nutrientsinclude Ascorbic Acid, pyruvate, and amino acids. A chondrogenesisinducing agent can include one or more of the materials as describedabove, for example a combination of TGF-β and pyruvate.

“Mesenchymal stem cells” or “MSCs” refers to multipotent stem cellscapable of differentiating into osteoblasts, chondrocytes, myocytes,adipocytes, neuronal cells, pancreatic islet cells, and the like.Additionally, methods and compositions detailing MSCs as described inU.S. Pat. Nos. 5,486,359, 6,387,367 and 5,197,985 are incorporated byreference herein in their entirety. In more detail, mesenchymal stemcells are multipotent stem cells located in the bone marrow, peripheralblood, adipose tissue and other like sources. Source MSCs of theinvention can be harvested from the iliac crest of the patient in need(or other source such as the IVD, periosteum, synovial fluid, or thevertebral body or pedicle) of the restorative/replacement therapy (or asuitable donor), such patient is referred to herein as a “patient inneed or patient in need thereof” (note that other sources, such asadipose tissue, synovial tissue, and connective tissue have recentlybeen identified and are also considered as MSC sources within the scopeof the present invention). In one embodiment, approximately 10-100 cc ofbone marrow is harvested and “isolated” using methods described in U.S.Patent Application 60/761,441 to Centeno or through adherence toplastic, as described in U.S. Pat. No. 5,486,359 to Caplan et al. Eachof these references is incorporated herein in their entirety for allpurposes.

“Platelet lysate” refers to the combination of natural growth factorscontained in platelets that have been released through lyses of theplatelets. Lyses can be accomplished through chemical means (i.e.,CaCl₂), osmotic means (use of distilled H₂O), or throughfreezing/thawing procedures. Platelet lysates of the invention can alsobe derived from whole blood and can be prepared as described in U.S.Pat. No. 5,198,357, which is incorporated by reference herein.

“Repair” refers to restoration of some or all of a surface's cartilageto an acceptable operating condition. In some instances this may entaila 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%,75%, 80%, 85%, 90%, 95%, 100%, and 100+% increase over the untreatedcondition in the patient in need of cartilage repair.

“Whole cell platelet concentrate”, “platelet rich plasma”, and “plateletrich fibrin” are as generally known in the art. For example, plateletrich plasma or PRP can be obtained through methods as described inLandesberg et al., J Oral Maxillogac Surg 58:297, 2000, which isincorporated by reference in its entirety.

Aspects of the Invention

Aspects of the present invention provide cartilage repair compositionsfor facilitating cartilage repair in a patient in need thereof.Embodiments include a therapeutically effective amount of plateletlysate in conjunction with one or more chondrogenesis inducing agents.In some cases the platelet lysate is an autologous platelet lysate. Insome cases the chondrogenesis inducing agent is an autologouschondrogenesis inducing agent.

In one embodiment, a repair composition includes a therapeuticallyeffective amount of one or more of a platelet rich plasma, platelet richfibrin, or a whole cell platelet concentrate in conjunction with one ormore chondrogenesis inducing agents. The platelet rich plasma, plateletrich fibrin and/or whole cell platelet concentrate can be autologous. Insome cases the platelet rich plasma, platelet rich fibrin and/or wholecell platelet concentrate can replace the platelet lysate. For purposesof the invention, any one or more of platelet lysate, platelet richplasma, platelet rich fibrin and/or whole cell platelet concentrate willbe referred to as a platelet-based material.

In another embodiment, the repair composition includes a therapeuticallyeffective amount of a combination of a platelet lysate and two or moreof platelet rich plasma, platelet rich fibrin or whole cell plateletconcentrate in conjunction with one or more chondrogenesis inducingagent(s). As above, either or both of the platelet lysate and two ormore of platelet rich plasma, platelet rich fibrin or whole cellplatelet concentrate can be autologous. In some embodiments thechondrogenesis inducing agent(s) is also autologous.

In still another embodiment, a repair composition of the inventionherein includes from about 10,0000 to 10,000,000,000 mesenchymal stemcells. In typical cases the mesenchymal stem cells are autologous andprepared per methods described in the definition section above or asdescribed in U.S. patent application Ser. No. 11,773,774 (and U.S.Provisional Patent Application No. 61/014,987), which are incorporatedherein by reference. Alternatively, about from 10,000 to 10,000,000,000chondrocytes can be combined with repair compositions of the invention,chondrocytes can be autologous. Autologous chondrocytes can be isolatedand expanded using techniques as described herein for MSCs as well asthrough a review of the relevant art, e.g., Johnson et al., TissueEngineering, 2004 10(9-10) 1308-1318, incorporated herein by reference.In other embodiments the mesenchymal stem cells or chondrocytes arenon-autologous and purchased from a vendor. In general, any combinationof cells useful for inclusion in the repair compositions herein will bereferred to as cell-based materials.

As such, repair compositions as described herein can include one or moreof the following: autologous or non-autologous platelet-basedmaterial(s); autologous or non-autologous chondrogenesis inducingagent(s); and autologous or non-autologous cell-based materials(s).

Other aspects of the present invention provide methods for facilitatingcartilage repair in a patient in need thereof.

Methods include, administering a repair composition (e.g., plateletlysate and chondrogenesis inducing agent) of the invention to a site ina patient in need of such therapy. Methods herein would includepreparation of the repair composition as either a autologous compositionor non-autologous composition. Where any one component of the repaircomposition is from a non-autologous source (excluding excipients,solutions, e.g., sterile PBS, and other materials required to administerthe repair composition) the entire composition is considerednon-autologous.

In another embodiment, the components that make up a repair compositioncan be administered sequentially, for example, the platelet lysate(and/or platelet rich plasma, platelet rich fibrin and/or whole cellplatelet concentrate) and chondrogenesis inducing agent can beadministered in a non-contemporaneous manner, for example within oneminute of each other, within ten minutes of each other, within one hourof each other, within one day of each other or within one week of eachother. Method embodiments herein include any administration procedurethat results in the components of the repair composition beingadministered to the site in need of repair, as long as theadministration is directed at repair of the same site in need of repairin the patient in need of repair.

In still other embodiments of the present invention, methods can includepreparing platelet lysate solutions, platelet rich plasma, platelet richfibrin and/or whole cell platelet concentrates from the patient in needof treatment. These platelet based materials are then autologous to thepatient in need of therapy. Methods for isolating and preparing thesematerials are described in U.S. patent application Ser. No. 11/773,774and U.S. Provisional Patent No. 61/014,987, which are incorporatedherein by reference for all uses.

As noted above, in some embodiments herein, mensenchymal stem cells areadministered in a therapeutic amount to the site in need of cartilagerepair either contemporaneously or non-contemporaneously with the repaircompositions of the invention.

Cartilage Repair Compositions

In more detail, composition embodiments of the invention includecartilage repair compositions having an enhanced capacity for cartilagerepair in a patient in need thereof. Cartilage repair compositionembodiments in accordance with the invention include variouscombinations of: platelet lysate solution, platelet rich fibrin,platelet rich plasma, and whole cell platelet concentrate with one ormore chonodrogenesis inducing agent(s). Chondrogenesis inducing agentsinclude various growth factors, cytokines, hormones and nutrients thathave been shown to induce or facilitate cartilage growth in the in vivoor in vitro setting.

In some embodiments, the platelet lysate solution, platelet rich fibrin,platelet rich plasma and/or whole cell platelet concentrate areautologous to the patient receiving the repair composition. In otherembodiments, the chondorgenesis inducing agent(s) is also autologous tothe patient receiving the repair composition.

Autologous platelet-based materials are harvested and prepared asdescribed in U.S. patent application Ser. No. 11/773,774, incorporatedherein by reference for all uses. Autologous chondrogenesis inducingagents are obtained per the target agent, for example, growth factorslike BMP-7 and BMP-2 can be purchased from Stryker, Inc and Medtronic,cytokines like entanercept (TNF-alpha inhibitor) can be purchased fromAmgen/Wyeth, Inc, and the like.

In typical embodiments the repair compositions include stem cell orcartilage cell growth enhancing compositions of autologous plateletlysate solution. The platelet lysate solution of the invention istypically from about 5% to about 40% plaelet lysate, and more typicallybetween about 5% and 20% platelet lysate. Optimal levels of plateletlysate for any given patient can be determined based on bioavailabilityand concentrations of growth factors in the patients lysate. Optimallevels can be determined by reference to U.S. patent application Ser.No. 11/773,774, incorporated herein by reference for all purposes.

Typical chondrogenesis inducing agents herein include growth factorsthat induce or facilitate cartilage growth. Growth factors include:fibroblast growth factor, insulin like growth factor-1, transforminggrowth factor-beta, bone morphogenetic protein-2, human growth hormone,PDGF-BB, and the like. (see for example: Cassiede et al., J Bone MinerRes., 1996. 11(9): p. 1264-73; Miyata et al., J Cell Physiol., 2005.204(3): p. 948-55; Kawamura et al., Exp Hematol., 2005. 33(8): p.865-72; Zhang et al., J Huazhong Univ Sci Technolog Med Sci., 2004.24(3): p. 275-8; Toh et al., Growth Factors, 2005. 23(4): p. 313-21;Chrisman, O. D., Clin Orthop Relat Res., 1975 (107): p. 232-8; Denko etal., Semin Arthritis Rheum, 2005. 35(1): p. 24-34, each of which isincorporated by references for all purposes herein). Illustrativeamounts of chondrogenesis inducing agents include: 1-100 ng/ml (1-500nM) dose of corticosteroid, 1-500 ng/ml of TGF-beta, 1-500 nM AscobicAcid (1-500 mg/ml), FGF-2 of 1-100 ng/mL, 10-500 ng/mL of IGF-I.

Other typical chondrogenesis inducing agents herein can includecytokines that induce or facilitate cartilage growth. Illustrativecytokines include: interleukin-1 (IL-1) and Cytokine-like 1 (Cyt11).Typical chondrogenesis inducing agents herein can also include steroidhormones like corticosteroid, human growth hormone, testosterone.

Note also that typical chondrogenesis inducing agents herein can includevarious cartilage inducing nutrients, for example: glucosamine,hyaluronic acid, (Zhu et al., Stem Cell 2005, incorporated by referenceherein for all purposes), collagen, glycoaminoglycans, amino acidmixtures, sodium pyruvate, ascorbic acid, carbohydrates, and thelike.(Cassiede et al.; Miyata et al.; Kawamura et al.; Zhang et al.; Tohet al.; Bosnakovski et al., Biotechnol Bioeng., 2006. 93(6): p. 1152-63;Derfoul et al., Osteoarthritis Cartilage, 2007. 15(6): p. 646-55; Songet al., Cytotherapy, 2004. 6(6): p. 596-601, each of which isincorporated by reference in its entirety for all purposes.). In someembodiments, combinations of one or more types of chondrogenesisinducing agents are combined with the platelet-based solutions of theinvention, for example: a growth factor in combination with a cytokine,a growth factor in combination with a nutrient, or other likecombinations.

In one embodiment, an about 5% to 40% platelet lysate solution iscombined with one or more chondrogeneis inducing agents. Illustrativechondorgenesis inducing agent combinations include IGF-1 andcorticosteroid with or without collagen. Platelet lysate with 50 ng/mlof dexamethasone, platelet lysate with ascorbic acid, dexamethasone, andpyrate, and the like.

In other repair composition embodiments, mesenchymal stem cells arecombined with the platelet-based solutions and chondrogenesis inducingagents of the invention. Mesenchymal stem cells are typically autologousand can be harvested and expanded from the patient in need thereof bythe methods described above. In alterative embodiments, chondrocytes arecombined with the platelet-based solutions and chondrogenesis inducingagents of the invention. Chondrocytes are typically autologous and canbe harvested and expanded from the patient in need thereof. In someembodiments a mix of mesenchymal stem cells and various differentiatedforms of mesenchymal stem cells (up to and including chondrocytes) arecombined with the platelet-based solutions and chondrogenesis inducingagents. Regardless of the nature of the cells, they can be expandedprior to implantation into the patient in need thereof in accordancewith aspects of the present invention.

In still other repair compositions, a carrier material is added tomodify the capacity of the embodiments to remain at the site of injuryor the timing of release of the composition into the site of injury.Illustrative carriers include: gels, hydrogels, foams, or likematerials. These carriers can be combined with the platelet-basedmaterials and chondrogenesis inducing agents with or without celladditives, e.g., mesenchymal stem cells, chondrocytes, etc of theinvention. In some aspects the carriers are incorporated as ascaffolding for cell additives or for endogenous cells (generallymesenchymal stem cells or chondrocytes) at or close to the site ofinjury.

As noted previously, repair compositions can be administered to a sitein need of repair as a single composition or sequentially, where eachcomponent of the composition is added at an appropriate time to maximizerepair.

Methods Of Inducing Or Facilitating Cartilage Repair In A Patient InNeed Thereof

Embodiments of the invention include therapeutic methods for restoringcartilage at a site in need of repair in a patient in need thereof. Forpurposes of the invention a site in need of repair is any site in amammal, e.g., human, horse, dog, etc., in need of cartilage repair orreplacement. An illustrative site is a knee joint in a patient havingosteoarthritis.

In one embodiment, an initial determination is made as to what type andhow much repair composition would be effective in treating the site inneed of repair. This determination is based on site of repair, age ofpatient, autologous or non-autologous platelet-based lysate, type andamount of chondrogenesis inducing agent, etc. A determination is alsomade as to the timing of delivery of the different aspects of the repaircomposition. For example, chondrogenesis inducing agents can be selectedfor their capacity for degranulation of platelets at an optimal timeafter administration to the patient. The correct timing in such casemust be determined, especially where the platelet-based composition isadministered at a time zero and the chondrogenesis inducing agent, e.g.,cytokine, is administered at a time X, X representing the optimal timeat which to have administered platelet materials degranulate. Variousaspects of this initial determination are described in PCT applicationPCT/US2008/087452, Compositions and methods to promote implantation andengraftment of stem cells, which is incorporated by reference herein forall purposes.

Once the above determinations have been made, methods herein requireadministration of repair compositions of the invention to the patient inneed thereof. Administration to the site in need of repair can beaccomplished through a surgical incision, arthroscopically, orpercutaneously.

Administration may be performed one or more times in order to maximizecartilage repair or replacement. Injury site analysis can be performedto ensure that acceptable results have been achieved.

Therapeutic Applications

Repair compositions of the invention provide optimal cartilage repairand/or replacement conditions/environment to repair a site in a patientin need thereof.

Repair compositions herein can be formulated as pharmaceuticalcompositions and administered to a patient in need thereof, typically amammalian, including a human patient. Repair compositions can beformulated in a variety of forms adapted for the chosen route ofadministration.

For administration of the compositions of the invention as an injectablesolution (whether it be through a surgical incision orarthroscopically), compositions can be formulated according totechniques well-known in the art, using suitable dispersing or wettingagents, such as sterile oils, including synthetic mono- or di-glyceridesand fatty acids, including oleic acid.

Solutions or suspensions of the repair compositions can be prepared inwater, isotonic saline (PBS), and optimally mixed with an nontoxicsurfactant. Dispersions may also be prepared in glycerol, liquidpolyethylene, glycols, vegetable oils, triacetin and mixtures thereof.Under customary use and storage conditions, the repair compositionsherein may contain one or more preservatives to prevent growth ofmicroorganisms.

“Therapeutic applications” herein refers to use of the compositions andmethods of the invention to treat a patient having a site in need ofcartilage repair or replacement. In some embodiments, the inventionsdisclosed herein include therapeutic applications in patients havingdisease states that limit the inherent ability of the patient to repairor re-grow cells at the repair site. For example, patient's that haveosteoarthritis.

The description of the present invention has been presented for purposesof illustration and description, but is not intended to be exhaustive orlimiting of the invention to the form disclosed. The scope of thepresent invention is limited only by the scope of the following claims.Many modifications and variations will be apparent to those of ordinaryskill in the art. The embodiment described and shown in the figures waschosen and described in order to best explain the principles of theinvention, the practical application, and to enable others of ordinaryskill in the art to understand the invention for various embodimentswith various modifications as are suited to the particular usecontemplated.

While the invention has been particularly shown and described withreference to a number of embodiments, it would be understood by thoseskilled in the art that changes in the form and details may be made tothe various embodiments disclosed herein without departing from thespirit and scope of the invention and that the various embodimentsdisclosed herein are not intended to act as limitations on the scope ofthe claims. All references cited herein are incorporated in theirentirety by reference.

-   1. Cassiede, P., et al., Osteochondrogenic potential of marrow    mesenchymal progenitor cells exposed to TGF-beta 1 or PDGF-BB as    assayed in vivo and in vitro. J Bone Miner Res, 1996. 11(9): p.    1264-73.-   2. Miyata, T., et al., Platelet-derived growth factor-BB (PDGF-BB)    induces differentiation of bone marrow endothelial progenitor    cell-derived cell line TR-BME2 into mural cells, and changes the    phenotype. J Cell Physiol, 2005. 204(3): p. 948-55.-   3. Kawamura, K., et al., Adenoviral-mediated transfer of TGF-beta1    but not IGF-1 induces chondrogenic differentiation of human    mesenchymal stem cells in pellet cultures. Exp Hematol, 2005.    33(8): p. 865-72.-   4. Zhang, Y., et al., In vitro chondrogenic phenotype    differentiation of bone marrow-derived mesenchymal stem cells. J    Huazhong Univ Sci Technolog Med Sci, 2004. 24(3): p. 275-8.-   5. Toh, W. S., et al., Combined effects of TGFbeta1 and BMP2 in    serum-free chondrogenic differentiation of mesenchymal stem cells    induced hyaline-like cartilage formation. Growth Factors, 2005.    23(4): p. 313-21.-   6. Chrisman, O. D., The effect of growth hormone on established    cartilage lesions. A presidential address to the Association of Bone    and Joint Surgeons, 1974. Clin Orthop Relat Res, 1975(107): p.    232-8.-   7. Denko, C. W. and C. J. Malemud, Role of the growth    hormone/insulin-like growth factor-1 paracrine axis in rheumatic    diseases. Semin Arthritis Rheum, 2005. 35(1): p. 24-34.-   8. Zhu, H., et al., The Role of the Hyaluronan Receptor CD44 in MSC    Migration in the

Extracellular Matrix. Stem Cells, 2005.

-   9. Bosnakovski, D., et al., Chondrogenic differentiation of bovine    bone marrow mesenchymal stem cells (MSCs) in different hydrogels:    influence of collagen type II extracellular matrix on MSC    chondrogenesis. Biotechnol Bioeng, 2006. 93(6): p. 1152-63.-   10. Derfoul, A., et al., Glucosamine promotes chondrogenic phenotype    in both chondrocytes and mesenchymal stem cells and inhibits MMP-13    expression and matrix degradation. Osteoarthritis Cartilage, 2007.    15(6): p. 646-55.-   11. Song, L., D. Baksh, and R. S. Tuan, Mesenchymal stem cell-based    cartilage tissue engineering: cells, scaffold and biology.    Cytotherapy, 2004. 6(6): p. 596-601.

All references herein are incorporated by reference for all purposes.

1. A composition for facilitating cartilage repair in a patient in needthereof comprising a therapeutically effective amount of an autologousplatelet lysate and one or more chondrogenesis inducing agents.
 2. Thecomposition of claim 1 wherein the platelet lysate is from about 5% toabout 40% platelet lysate solution.
 3. The composition of claim 1wherein the chondrogenesis inducing agent is one or more growth factors,one or more cytokines, one or more hormones, or one or more essentialnutrients.
 4. The composition of claim 3 wherein the chondrogenesisinducing agent is a hormone and wherein the hormone is corticosteroid.5. The composition of claim 3 wherein the chondrogenesis inducing agentis a growth factor and wherein the growth factor is transforming growthfactor β, fibroblast growth factor or a bone morphogenetic protein. 6.The composition of claim 3 wherein the chondrogenesis inducing agent isa cytokine and wherein the cytokine is IL-1.
 7. The composition of claim3 wherein the chondrogenesis inducing agent is an essential nutrient andwherein the essential nutrient is ascorbic acid, collagen, amino acids,peptides, sodium pyruvate, glucose, glutamine, ribonucleosides,carbohydrates, essential oils or deoxyribonucleosides.
 8. Thecomposition of claim 1 further comprising platelet rich plasma, plateletrich fibrin, whole cell platelets or a mixture thereof.
 9. Thecomposition of claim 1 further comprising a gel, hydrogel, foam, orother carrier material.
 10. A method for facilitating cartilage repairin a patient in need thereof comprising: obtaining platelets from thepatient; preparing a 5% to 40% platelet lysate solution from theplatelets; obtaining one or more chondrogenesis inducing agents; andadministering the 5% to 40% platelet lysate solution and chondrogenesisinducing agent to a site in the patient in need of cartilage repair;wherein the combined administration of the 5 to 40% platelet lysatesolution and chondrogenesis inducing agent facilitates cartilage repairat the site in the patient in need of repair.
 11. The method of claim 10wherein the chondrogenesis inducing agent is one or more growth factors,one or more cytokines, one or more hormones, or one or more essentialnutrients.
 12. The method of claim 10 further comprising administering aplatelet rich plasma, platelet rich fibrin, whole cell platelet or amixtures thereof to the patient in need thereof wherein theadministration is at the site in the patient in need of repair.